Lanaform Medi Stim Mode D'emploi page 18

EN
FR NL
GUIDANCE AND MANUFACTURER'S DECLARATION :
ELECTROMAGNETIC IMMUNITY
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment.
Immunity test
Electrostatic
discharge (ESD)
lEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
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M-MediStim-001.indd 18
IEC 60601
Compliance level Electromagnetic environment guidance
test level
±6 kV contact ±6 kV contact
±8 kV air ±8 kV air
±2 kV for power
Not applicable
supply lines
±1kV differential
mode
Not applicable
±2kV common
mode
<5% UT (>95% dip
in UT) for 0.5 cycle
40% UT (60% dip
in UT) for 5 cycles
Not applicable
70% UT (30% dip
in UT) for 25 cycles
<5% UT (>95% dip
in UT) for 5 sec
3A/m 3A/m
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the relative
humidity should be at least 30%. If ESD interfere with
the operation of equipment, counter measurements
such as wrist strap, grounding shall be considered.
Mains power quality should be that of a typical
commercial or hospital environment.
Mains power quality should be that of a typical
commercial or hospital environment.
Mains power quality should be that of typical commercial
or hospital environment. If the user of the device requires
continued operation during power mains interruptions,
it is recommended that the devices be powered
from an uninterruptible power supply or a battery.
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
19/12/2017 14:45:35